Expression of nuclear factor -κBp65 in mononuclear cells in Kawasaki disease and its relation to coronary artery lesions
- PMID: 21688043
- DOI: 10.1007/s12098-011-0478-x
Expression of nuclear factor -κBp65 in mononuclear cells in Kawasaki disease and its relation to coronary artery lesions
Abstract
Objective: To assess the association of nuclear factor-kappa B (NF-κB) and complications of Kawasaki disease (KD) in Chinese children.
Methods: Based on color Doppler examination results, 86 affected children in the KD group were divided into two groups: 39 cases in coronary artery lesion group (CALs subgroup) and 47 cases in non-coronary artery lesion group (Non-CALs subgroup). Infection control group consisted of 65 cases of hospitalized infected children with fever, having same age as the affected children. Healthy control group consisted of 102 cases of healthy children of the same age, visiting the hospital for physical examination. Western blot was used to detect the expression of NF-кBp65 and IкBα proteins in periphery blood mononuclear cells (PBMC); reverse transcription polymerase chain reaction (RT-PCR) was used to detect the expression of TNF-α and MCP-1 mRNA.
Results: The value of NF-kBp65 (optical density) in the PBMC cell nuclei in the KD group was significantly higher than that in the two control groups (p < 0.01). The value of NF-κBp65 in the CALs subgroup was significantly higher than that in the Non-CALs subgroup (p < 0.05). The value of NF-κBp65 inhibitor IκBα in the KD group was significantly lower than that in the infection control group and the healthy control group (p < 0.01). There was a positive correlation between the ratio nucleus NF-κBP65/ IκBα and the severity degree of CALs(r = 0.536, p < 0.05). The value of TNF-α mRNA (O.D ratio) in the KD group was significantly higher than that in the two control groups (P < 0.01), and the value of TNF-α mRNA in the CALs subgroup was significantly higher than that in the Non-CALs subgroup (P < 0.05). The value of MCP-1 mRNA in the KD group was significantly higher than that in the two control groups (P < 0.01), and the value of MCP-1 mRNA in the CALs subgroup was significantly higher than that in the Non-CALs subgroup (P < 0.05).
Conclusions: NF-κBp65 participates in the pathogenesis of vasculitis of KD in acute stage, and may aggravate the vasculitis in KD and plays a part in the formation of CALs.
Similar articles
-
Activated partial thromboplastin time levels and coronary artery lesions in Kawasaki disease: A retrospective cohort study.Microvasc Res. 2025 Jul;160:104817. doi: 10.1016/j.mvr.2025.104817. Epub 2025 May 7. Microvasc Res. 2025. PMID: 40345320
-
Plasma proteomic profiling reveals that SERPINE1 is a potential biomarker associated with coronary artery lesions in Kawasaki disease.Int Immunopharmacol. 2024 Sep 30;139:112698. doi: 10.1016/j.intimp.2024.112698. Epub 2024 Jul 18. Int Immunopharmacol. 2024. PMID: 39029232
-
Diagnostic value of syndecan-1 for coronary artery lesions and correlation analysis of laboratory indicators in Kawasaki disease patients.Ital J Pediatr. 2024 Oct 9;50(1):209. doi: 10.1186/s13052-024-01772-0. Ital J Pediatr. 2024. PMID: 39385218 Free PMC article.
-
Diagnostic significance of circulating miRNAs in Kawasaki disease in China: Current evidence based on a meta-analysis.Medicine (Baltimore). 2021 Feb 12;100(6):e24174. doi: 10.1097/MD.0000000000024174. Medicine (Baltimore). 2021. PMID: 33578520 Free PMC article.
-
[Recent research on the nuclear factor-kappa B signaling pathway in cardiac injury in children with Kawasaki disease].Zhongguo Dang Dai Er Ke Za Zhi. 2023 Mar 15;25(3):250-252. doi: 10.7499/j.issn.1008-8830.2209008. Zhongguo Dang Dai Er Ke Za Zhi. 2023. PMID: 36946158 Free PMC article. Review. Chinese.
Cited by
-
Prediction of the risk of coronary arterial lesions in Kawasaki disease by serum 25-hydroxyvitamin D3.Eur J Pediatr. 2014 Nov;173(11):1467-71. doi: 10.1007/s00431-014-2346-y. Epub 2014 Jun 3. Eur J Pediatr. 2014. PMID: 24889335 Free PMC article.
-
Can data from paediatric cohorts solve the COVID-19 puzzle?PLoS Pathog. 2020 Sep 9;16(9):e1008798. doi: 10.1371/journal.ppat.1008798. eCollection 2020 Sep. PLoS Pathog. 2020. PMID: 32903279 Free PMC article. Review.
-
KCa3.1 Inhibition of Macrophages Suppresses Inflammatory Response Leading to Endothelial Damage in a Cell Model of Kawasaki Disease.J Inflamm Res. 2021 Mar 5;14:719-735. doi: 10.2147/JIR.S297131. eCollection 2021. J Inflamm Res. 2021. PMID: 33727847 Free PMC article.
-
Understanding the pathogenesis of Kawasaki disease by network and pathway analysis.Comput Math Methods Med. 2013;2013:989307. doi: 10.1155/2013/989307. Epub 2013 Mar 6. Comput Math Methods Med. 2013. PMID: 23533546 Free PMC article. Review.
-
[Research advances in association between vitamin D and Kawasaki disease and related mechanisms of action].Zhongguo Dang Dai Er Ke Za Zhi. 2016 Dec;18(12):1319-1323. doi: 10.7499/j.issn.1008-8830.2016.12.024. Zhongguo Dang Dai Er Ke Za Zhi. 2016. PMID: 27974130 Free PMC article. Review. Chinese.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials
Miscellaneous